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Completed

NCT Number: NCT02362958

A Multi-Center Study of Lapatinib in Patients With Trastuzumab-refractory Metastatic Breast Cancer

Evaluating the Efficacy of Lapatinib in Combination With Chemotherapy in Patients With Trastuzumab-refractory Metastatic HER2-positive Breast Cancer.

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Key information

Age range

18 year–65 year

Sex eligibility

Female

Study type

Interventional

Phase

Phase 2

Primary location

Sun Yat-sen University Cancer Center

Guangzhou, Guangdong, 510080, China

About this study

Some studies has demonstrated that even in trastuzumab pretreated patients with HER-2 positive breast cancer, might benefit from the treatment of trastuzumab. However, there is small benefit for some patients having short disease-free survival after adjuvant trastuzumab or short progression-free survival after first-line trastuzumab-based therapy. In clinical practice, the investigators also found it is fact. And the investigators have a scientific rationale for clinical testing of lapatinib plus chemotherapy in patients with trastuzumab-refractory, metastatic HER2-positive breast cancer.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Metastatic breast cancer
  • Eastern Cooperative Oncology Group (ECOG) 0 or 1
  • HER2-expressing primary or metastatic tumor
  • Recurrence within 1 year completing adjuvant trastuzumab OR rapid progress following first-line trastuzumab-based care.
  • Measurable disease with Response Evaluation Criteria in Solid Tumors (RECIST) 1.1
  • Normal organ function, including bone marrow function, renal function, liver function, and cardiac function
  • Signed and dated an informed consent form
  • Life expectancy of at least 12 weeks

Exclusion criteria

  • Pregnant or breast feeding
  • left ventricular ejection fraction (LVEF) < 45% by echocardiogram
  • Disease-free interval (DFI) less than 12 months
  • Uncontrolled medical problems
  • Any previous malignancy exceptions for carcinoma of the cervix, squamous carcinoma of the skin, or basal cell carcinoma of the skin
  • Patients were unable or unwilling to comply with program requirements

Treatment and study plan

lapatinib and capecitabine or vinorelbine

Drug

lapatinib 1250 mg qd and Capecitabine 1000 mg/m2 bid or Vinorelbine 25mg/m2(d1,d8)

Other names: Tykerb; Xeloda;NVB

Primary outcomes

  1. progression-free survival

    Time frame: 36 months

    The time from randomization to disease progression or death from any causes

Sponsors and collaborators

Lead sponsor

Sun Yat-sen University

Other

Registry information

Official study title

Sun Yat-sen University Cancer Center

Important dates

Study start
2015
Primary completion
2020
Study completion
2020
First posted
Feb 13, 2015
Registry last updated
Jul 15, 2020

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.